What does aseptic processing in pharmaceutical manufacturing aim to achieve?

Aseptic processing in pharmaceutical manufacturing is primarily focused on making a product sterile by preventing contamination. This technique involves creating an environment free from microorganisms to ensure that the final pharmaceutical product is safe for use. Contamination can occur from various sources, such as the air, equipment, or even the personnel involved in the manufacturing process. By implementing aseptic processing techniques, manufacturers can effectively safeguard the quality and efficacy of the drug, providing a product that meets stringent health and regulatory standards.

In this context, aseptic processing is crucial for products such as injectables, which must be sterile to protect patient health. The process employs various strategies, including sterilization of materials, using clean rooms, and maintaining strict control over environmental conditions to mitigate the risk of contamination. Thus, the central aim of aseptic processing is to ensure the sterility of the product, making option B the correct choice.